Spinal Dysraphism and MalformationsFolate and B Vitamins ResearchTeratomas and Epidermoid Cysts

Chebet Frida, Hussein Ayub Maiga, Oloya Johnson Nyeko, Kiryowa Haruna, Catherine Lutalo Mwesigwa, Ochieng Joseph

2026.1.1East African Journal of Neurological Sciences

DOI: 10.4314/eajns.v5i2.6

Abstract

Background: Spina bifida, a neural tube defect, continues to pose substantial public health challenges in Uganda despite multiple preventive efforts. An estimated 1,400 children are affected annually. We conducted a retrospective cross-sectional review of hospital records for children diagnosed with spina bifida between 2020 and 2023. Methods: Using systematic sampling, we selected 414 patient records. We analysed the data using SPSS version 20. We defined severe spina bifida as a lumbosacral lesion presenting clinically with hydrocephalus. Results: Males constituted 60.4% of cases (n=250). Infants aged <1 year comprised 36.2% (n=150). Most lesions (69.0%) were located in the lumbosacral region; sacral lesions accounted for 17.4%, lumbar 8.0%, lumbothoracic 4.6%, and occipital and cervical regions 0.5% each. Regarding lesion integrity, the highest proportion of intact lesions occurred in the lumbosacral region (48.1%), followed by sacral (16.2%), lumbar (15.2%), and lumbothoracic (12.4%); ruptured lesions were also observed in the thoracic region (7.8%). Maternal febrile illness was associated with severe spina bifida (adjusted OR 2.24, 95% CI 1.34–3.74; p=0.02). Tertiary maternal education was also associated with higher odds of spina bifida (adjusted OR 2.27, 95% CI 1.43–4.57; p=0.01). Conclusion: Myelomeningocele remains the predominant form of spina bifida in Uganda, chiefly affecting the lumbosacral region.

Citation format

FRIDA, Chebet, et al. Anatomical characteristics, clinical features, and risk factors of spina bifida: A retrospective review of children at cure hospital, uganda. East African Journal of Neurological Sciences, 2026, 5(2): 100–106.